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N-[2-(tert-butyl-dimethyl-silanyloxy)-1-formyl-ethyl]-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

503560-10-9

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503560-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503560-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,5,6 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 503560-10:
(8*5)+(7*0)+(6*3)+(5*5)+(4*6)+(3*0)+(2*1)+(1*0)=109
109 % 10 = 9
So 503560-10-9 is a valid CAS Registry Number.

503560-10-9Upstream product

503560-10-9Relevant academic research and scientific papers

Total synthesis of sphingofungin F.

Lee, Kee-Young,Oh, Chang-Young,Ham, Won-Hun

, p. 4403 - 4405 (2002)

[reaction: see text] A concise, stereocontrolled synthesis of sphingofungin F was achieved. Key features involve diastereoselective oxazoline formation catalyzed by palladium(0), MgBr(2)-promoted gamma-alkoxy allylic stannane addition, and palladium(0)-ca

Stereoselective intramolecular cyclization of isopentenyl benzamide via π-allylpalladium complex catalyzed by Pd(0)

Joo, Jae-Eun,Mu, Yu,Lee, Yiu-Suk,Tian, Yong-Shou,Lee, Gyu-Jin,Ham, Won-Hun

experimental part, p. 293 - 304 (2010/08/20)

An efficient procedure was developed to synthesize oxazoline as key intermediate in the total synthesis of (+)-lactacystin using palladium(0)-catalyzed intramolecular cyclization of isopentenyl benzamide via a π-allylpalladium complex. A convenient and ef

Stereoselective synthesis of (+)-spectaline

Lee, Yiu-Suk,Shin, Yong-Ho,Kim, Yong-Hyun,Lee, Kee-Young,Oh, Chang-Young,Pyun, Sung-Jae,Park, Hyun-Ju,Jeong, Jin-Hyun,Ham, Won-Hun

, p. 87 - 93 (2007/10/03)

Our synthesis of (+)-spectaline revealed that the methodology involving diastereoselective palladium(0)-catalyzed oxazoline formation and intramolecular reductive amination by catalytic hydrogenation of an oxazoline is an effective method for the asymmetric synthesis of natural products possessing complex functionalized piperidine cores.

Total synthesis of myriocin

Lee, Kee-Young,Oh, Chang-Young,Kim, Yong-Hyun,Joo, Jae-Eun,Ham, Won-Hun

, p. 9361 - 9363 (2007/10/03)

A concise, stereocontrolled synthesis of myriocin was achieved. Key features involve diastereoselective oxazoline formation catalyzed by palladium(0), MgBr2-promoted allylic stannane addition, and palladium(0)-catalyzed coupling of a vinyl iodide with an organozinc reagent.

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